Allele Registry

Canonical Allele Identifier: PA2830325857

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000518408

RCV000653844

ClinVar Variation:

447702

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg41Leu	CA342807753 NM_170707.4:c.122G>T